Boyer Laurie A, Lee Tong Ihn, Cole Megan F, Johnstone Sarah E, Levine Stuart S, Zucker Jacob P, Guenther Matthew G, Kumar Roshan M, Murray Heather L, Jenner Richard G, Gifford David K, Melton Douglas A, Jaenisch Rudolf, Young Richard A
Whitehead Institute for Biomedical Research, 9 Cambridge Center, Cambridge, Massachusetts 02142, USA.
Cell. 2005 Sep 23;122(6):947-56. doi: 10.1016/j.cell.2005.08.020.
The transcription factors OCT4, SOX2, and NANOG have essential roles in early development and are required for the propagation of undifferentiated embryonic stem (ES) cells in culture. To gain insights into transcriptional regulation of human ES cells, we have identified OCT4, SOX2, and NANOG target genes using genome-scale location analysis. We found, surprisingly, that OCT4, SOX2, and NANOG co-occupy a substantial portion of their target genes. These target genes frequently encode transcription factors, many of which are developmentally important homeodomain proteins. Our data also indicate that OCT4, SOX2, and NANOG collaborate to form regulatory circuitry consisting of autoregulatory and feedforward loops. These results provide new insights into the transcriptional regulation of stem cells and reveal how OCT4, SOX2, and NANOG contribute to pluripotency and self-renewal.
转录因子OCT4、SOX2和NANOG在早期发育中起关键作用,并且是培养中未分化胚胎干细胞增殖所必需的。为了深入了解人类胚胎干细胞的转录调控,我们使用基因组规模定位分析鉴定了OCT4、SOX2和NANOG的靶基因。令人惊讶的是,我们发现OCT4、SOX2和NANOG共同占据了它们靶基因的很大一部分。这些靶基因经常编码转录因子,其中许多是在发育中起重要作用的同源域蛋白。我们的数据还表明,OCT4、SOX2和NANOG协同作用形成由自调控和前馈环组成的调控回路。这些结果为干细胞的转录调控提供了新的见解,并揭示了OCT4、SOX2和NANOG如何促进多能性和自我更新。